FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Device, Thermal Ablation, Endometrial
PMA: P010013
·
Supplement: S070
·
Decision May 17, 2018
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Device, Thermal Ablation, Endometrial
- Trade Name
- NovaSure Impedance Controlled Endometrail Ablation Device
- PMA Number
- P010013
- Supplement Number
- S070
- Device Class
- FDA Class 3
- Product Code
- MNB
- Generic Name
- Device, thermal ablation, endometrial
- Medical Specialty
- Unknown
- Advisory Committee
- Obstetrics/Gynecology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- May 17, 2018
- Date Received
- April 19, 2018
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Addition of the second supplier for the Thumb Pusher Component of the Novasure Disposable Device and the addition of the second supplier for the CO2 Cartridge 5-Pack Assembly.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MNB | Device, Thermal Ablation, Endometrial | FDA class 3 | Unknown |